2,3-Dichloro-5-formylpyridine

    • Product Name: 2,3-Dichloro-5-formylpyridine
    • Chemical Name (IUPAC): 2,3-dichloro-5-formylpyridine
    • CAS No.: 875781-17-2
    • Chemical Formula: C6H3Cl2NO
    • Form/Physical State: Powder to crystalline
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    804850

    Chemical Name 2,3-Dichloro-5-formylpyridine
    Cas Number 6968-76-3
    Molecular Formula C6H3Cl2NO
    Molecular Weight 176.00 g/mol
    Appearance Off-white to pale yellow solid
    Melting Point 63-66°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO, DMF
    Smiles C1=C(C=NC(=C1Cl)Cl)C=O
    Inchi InChI=1S/C6H3Cl2NO/c7-5-4(3-10)1-2-9-6(5)8
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 5-Formyl-2,3-dichloropyridine

    As an accredited 2,3-Dichloro-5-formylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, labeled “2,3-Dichloro-5-formylpyridine,” featuring hazard and handling information.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 160 drums (each 200 kg) of 2,3-Dichloro-5-formylpyridine, total net weight 32,000 kg.
    Shipping 2,3-Dichloro-5-formylpyridine is shipped in tightly sealed containers, protected from light, moisture, and heat. It is packaged according to regulations for hazardous chemicals, with clear labeling and safety documentation included. Handling and transport comply with relevant local and international chemical shipping guidelines to ensure safe and secure delivery.
    Storage Store 2,3-Dichloro-5-formylpyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Keep it away from heat and ignition sources. Use appropriate corrosion-resistant containers and ensure proper chemical labeling. Access should be limited to trained personnel with proper personal protective equipment (PPE).
    Shelf Life 2,3-Dichloro-5-formylpyridine is stable under recommended storage conditions, typically has a shelf life of at least two years.
    Application of 2,3-Dichloro-5-formylpyridine

    Purity 98%: 2,3-Dichloro-5-formylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation.

    Melting Point 103-106°C: 2,3-Dichloro-5-formylpyridine with a melting point of 103-106°C is used in fine chemical manufacturing, where it provides thermal stability during process scaling.

    Molecular Weight 178.00 g/mol: 2,3-Dichloro-5-formylpyridine with a molecular weight of 178.00 g/mol is used in agrochemical research, where it enables precise molecular incorporation in target compounds.

    Solubility in DMSO: 2,3-Dichloro-5-formylpyridine with high solubility in DMSO is used in compound screening assays, where it facilitates homogeneous reaction solutions.

    Moisture Content <0.5%: 2,3-Dichloro-5-formylpyridine with moisture content below 0.5% is used in organometallic synthesis, where it helps prevent undesirable hydrolysis reactions.

    Particle Size <100 μm: 2,3-Dichloro-5-formylpyridine with particle size under 100 μm is used in solid-phase chemical processing, where it enables uniform blend and reactivity.

    Stability Temperature up to 80°C: 2,3-Dichloro-5-formylpyridine with stability temperature up to 80°C is used in heated batch reactors, where it maintains chemical integrity under process temperatures.

    Chromatographic Purity >99%: 2,3-Dichloro-5-formylpyridine with chromatographic purity above 99% is used in analytical reference standards, where it ensures accurate and reproducible analyses.

    Low Residual Solvent Content: 2,3-Dichloro-5-formylpyridine with low residual solvent content is used in API synthesis, where it aids compliance with regulatory purity standards.

    High Chemical Reactivity: 2,3-Dichloro-5-formylpyridine with high chemical reactivity is used in aldehyde coupling reactions, where it improves reaction efficiency and conversion rates.

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    Certification & Compliance
    More Introduction

    Introducing 2,3-Dichloro-5-formylpyridine: A Modern Synthetic Building Block

    A Closer Look at an Unassuming but Essential Compound

    Everyone in the chemical and pharmaceutical world bumps into familiar names: big molecules, flashy catalysts, all the talk about “blockbusters.” Underneath that buzz, compounds like 2,3-Dichloro-5-formylpyridine do real work. This molecule, with its two chlorine atoms and a formyl group sitting neatly on a pyridine ring, does not grab attention in the same way. Yet, ask anyone in chemical synthesis or pharmaceutical development, and the respect for such building blocks becomes obvious. Having spent years in labs and dealing with the nitty-gritty of custom synthesis, I can say that reliable chemicals like this one make or break entire projects.

    What Sets 2,3-Dichloro-5-formylpyridine Apart

    It comes down to predictable performance and flexibility. In a market flooded with “me too” compounds, this one always offers something different. The backbone—a chlorinated pyridine—gives it a nice balance of reactivity and selectivity. Chemists rely on those positions; the two chlorine atoms activate the ring at the right places while leaving room for careful substitution. The formyl group—the business end—allows further modification, making it a solid stepping stone toward more complex molecules.

    Plenty of other pyridine derivatives exist, but most do not offer the same handle for downstream reactions. Take 2,3,5-trichloropyridine: it lines up three chlorines, but with no functional handle, it’s about as reactive as cold soup. Others, such as 3,5-dichloropyridine, lose much of the flexibility of formyl-substitution, forcing you down a limited path of synthesis. With 2,3-Dichloro-5-formylpyridine, you hold a practical key for further chemistry—especially valuable in intermediate steps when optimizing for selectivity or purification.

    Practical Utility in Research and Development

    Over the years, I have watched research teams struggle with batches of intermediates that fall short in quality or consistency. One lesson stands out: do not underestimate simple, versatile chemicals. 2,3-Dichloro-5-formylpyridine shows its value in medicinal chemistry programs where custom substitutions drive hits and leads in drug discovery. The formyl group, for instance, acts as a gateway to a whole host of downstream chemistries—whether that means reductive amination, condensation reactions, or Wittig transformations. That sort of headroom gives R&D more room to maneuver. The pyridine ring sits at the sweet spot: aromatic enough for stability, but reactive at precisely tuned sites, thanks to well-placed chlorines.

    Synthetic chemists, especially those chasing new heterocyclic cores or tailoring structure-activity relationships, need predictable—and high-purity—sources. Over time, and with repeated use, I’ve learned certain batches from reputable sources create fewer purification headaches. Consistency in melting point, solubility, and impurity profile matters. Labs that trust their source for this compound avoid wasted time with column chromatography, unexpected byproducts, or loss in yields, keeping projects on track and on budget.

    Making Ends Meet in a Tough Synthesis

    Everyone in process chemistry hits a wall: a step that should be easy hits some roadblock—a yield drop, impurity spike, or costly workup. If you work on a process route for an active pharmaceutical ingredient, having a reliable supply of the key intermediate pays off. 2,3-Dichloro-5-formylpyridine offers a dependable route to building more complex molecules. Those two electron-withdrawing chlorines can guide ortho/para selectivity, while the formyl group opens the door to forming new carbon–carbon or carbon–nitrogen bonds without the extra steps required by less functionalized analogues.

    This predictability is not just a technical detail—it keeps manufacturing schedules honest. If your intermediate batch fails to meet spec, you face delays and mounting costs. Anyone scaling up a process from milligrams in a lab notebook to kilos knows the pain of impurities that sneak past analytical methods at first but later clog up downstream purification. With this compound, years of experience show that, given correct storage, purity holds up and shelf life remains solid—nothing trashes months of work faster than a decomposed intermediate.

    Applications in Pharmaceutical and Agrochemical Synthesis

    In the realm of active ingredient synthesis for medicines or crop protection, precision matters. That’s where 2,3-Dichloro-5-formylpyridine elbowed its way onto the bench. Medicinal chemists lean on this scaffold for its rich transformation possibilities. Often, a synthetic scheme can involve modifying the formyl group, introducing diverse substituents which guide biological activity—tiny changes on a molecule that shift a compound from inactive to blockbuster.

    For agrochemicals, where volume and reliability take center stage, robustness matters just as much as reactivity. The demand for products handling pests or weeds in the field hinges on affordable, reproducible chemistry. 2,3-Dichloro-5-formylpyridine, with its stable structure, lets process chemists scale batches to meet cropping seasons or regulatory needs. It stands up well under standard storage, and the established synthesis routes give it a cost advantage over less accessible intermediates that often require esoteric raw materials or costly purification steps.

    My own corrections bench has seen more than a few failed reactions with less robust analogues. Yet, whenever we swapped in this compound, not only did our yields hold, but also our downstream separation chores dropped, as its profile avoided the worst of side reactions and stubborn byproducts. That makes a difference if you need a usable product, not just an academic demonstration.

    Comparison: Not All Pyridine Derivatives Are Created Equal

    Some might expect that swapping out one pyridine derivative for another would not matter much. Years in the lab show this just isn’t true. Many analogues either lack the same balance of reactivity or introduce new headaches by being less stable in air or light, or more sensitive to trace moisture. Some alternatives bring high cost or unpredictable handling—you open a drum and wind up with a clumpy, half-decomposed mess. Nothing halts a plant faster than a failed raw material.

    I’ve worked with relatives like 2-chloro-5-formylpyridine, which lack that dual activation pattern afforded by two adjacent chlorines. Those single-chlorine analogues behave just differently enough to force you back to the drawing board or to double your optimization efforts. The dual-chlorine motif of 2,3-Dichloro-5-formylpyridine means reactions like nucleophilic substitution, Suzuki-Miyaura coupling, or selective reductions proceed with fewer surprises. Process teams notice: you can largely rely on published methods working as described, saving time and troubleshooting.

    Quality and Safety: Lessons from Real-World Handling

    Quality counts in the chemical world; a product’s value drops if it cannot be trusted on the bench or at scale. Speaking plainly, nobody wants to repeat a step ten times just because one raw material gives off-spec results. 2,3-Dichloro-5-formylpyridine delivers because the community has honed reliable methods of both synthesis and purification. Rigorous analytical checks on each batch—think high-performance liquid chromatography, NMR, and GC-MS—help ensure you’re not introducing problems into later steps. Much of that comes from raw experience: a tighter impurity profile means fewer unplanned column runs, cleaner crystallizations, and less scavenging in the final product.

    Handling this compound fits neatly with standard protocols: use proper storage and avoid direct breathing of dust or fumes, just like with any other pyridine derivative. No outsized hazards, unlike some polychlorinated species, and a clear record of safe shipping and storage in standard containers. Users appreciate the predictability both in small-scale research settings and in larger industrial warehouses.

    Purity as a Differentiator

    One lesson keeps popping up in chemical work: a reagent needs to be as pure as advertised, or you learn the hard way. With 2,3-Dichloro-5-formylpyridine, you rarely see discrepancies between the label and reality. Suppliers who consistently deliver material at over 98% purity, with well-documented impurity profiles, win repeat business for a reason.

    Some competitive products falter by cutting corners on purification—leaving trace metals, solvent residues, or closely related side-products. These ghosts show up on chromatograms, spiking analytics and making scale-up a guessing game. The trust built by high-purity batches keeps whole teams moving forward, sparing everyone lengthy recrystallizations and lost weekends. I still remember one project where low-grade material forced us to spend weeks identifying a single trace impurity; switching to higher-purity 2,3-Dichloro-5-formylpyridine closed the case overnight.

    Driving Innovation in Heterocyclic Chemistry

    Cutting-edge research often depends on getting the details right at the molecular level. This compound opens up options for novel heterocycle synthesis—particularly fused pyridine systems, which underpin new drugs, dyes, and catalysts. Chemists who experiment with unusual coupling reactions or functional group interconversions appreciate how much versatility comes from a handle like the formyl group, especially against a backdrop of dual chlorines.

    Young researchers, eager to publish and patent new molecules, chase new coupling partners. Having 2,3-Dichloro-5-formylpyridine in the toolkit means they do not need to redesign routes from scratch or risk unreliable reactions. In a time crunch, reliable access to robust, well-characterized materials cuts project time and supports innovation. From early-stage discovery through optimization to pilot-scale trials, dependable intermediates free up researchers to push boundaries without fearing surprises from their building blocks.

    Environmental Responsibility and Handling Practices

    Chemical stewardship can’t be taken lightly. Unlike some legacy intermediates that hang around in the environment or break down into worrisome byproducts, 2,3-Dichloro-5-formylpyridine offers a simpler profile. Waste streams from its use are easier to manage because its chemistry is well-mapped, aiding safe disposal in line with routine protocols. Over the years, industry practice has built up a base of knowledge for safe handling, routine spill cleanup, and compliant waste management—a reality that supports responsible chemistry and public trust.

    On-site, safe storage—dry, cool, away from strong acids or oxidizers—keeps the material predictable. Companies building green processes find it easier to integrate this compound thanks to its well-audited profile and less demanding disposal steps, compared to some nitrogen- or phosphorus-heavy intermediates. Seasoned operators add straightforward controls to keep the workspace safe and processes straightforward—qualities valued both by line chemists and company safety officers.

    Supply Chain Reliability in Today’s Market

    In recent years, global supply chains faced stress from all angles—pandemic disruptions, changing tariffs, shipping bottlenecks. For specialty intermediates, uncertainty can grind production to a halt. 2,3-Dichloro-5-formylpyridine takes away some of that headache, thanks to established production in multiple regions and a base of trusted suppliers. Getting reliable, on-time delivery keeps both pharma and agrochemical manufacture moving.

    Having seen firsthand the effects of delayed or unpredictable shipments on process chemistry, I appreciate how a strong supplier network using well-honed manufacturing routes adds resilience. Teams that lock in reliable shipments reduce their exposure to urgent, last-minute substitutions and the risk of expensive rush charges or quality compromises. In the end, access to this compound supports not only individual lab programs, but whole production lines.

    Looking Ahead: This Intermediates’ Role in Future Synthesis

    As fields like medicinal chemistry, materials science, and agrochemicals push for more speed and flexibility, building blocks like 2,3-Dichloro-5-formylpyridine will only grow in importance. The ongoing hunt for better medicines and smarter agrochemicals means new substitutions and coupling strategies keep evolving. A molecule with clear, reliable handles maximizes synthetic efficiency, makes screening easier, and cuts out time lost to troubleshooting. This is not glamorous work, but the repeatable dependability of core reagents winds up driving breakthroughs that change people’s lives.

    To sum up what years in the field have taught: simple, versatile, well-characterized intermediates are the lifeblood of modern synthesis. 2,3-Dichloro-5-formylpyridine brings together those traits, giving researchers and process scientists a reliable edge. In a world where margins are thin and deadlines tight, a quality chemical makes all the difference—from the test tube to the hundred-liter reactor. Those aiming to shorten development cycles, control cost, and drive sustainable innovation can appreciate the humble precision of a proven intermediate.